Welcome to LookChem.com Sign In|Join Free

CAS

  • or

4250-38-8

Post Buying Request

4250-38-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4250-38-8 Usage

Uses

Nonacosanoic Acid (cas# 4250-38-8) is a useful analytical reagent for studying soil fatty acids.

Definition

ChEBI: A very long-chain fatty acid comprising of 29 carbon atoms.

Check Digit Verification of cas no

The CAS Registry Mumber 4250-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4250-38:
(6*4)+(5*2)+(4*5)+(3*0)+(2*3)+(1*8)=68
68 % 10 = 8
So 4250-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C29H58O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29(30)31/h2-28H2,1H3,(H,30,31)

4250-38-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name nonacosanoic acid

1.2 Other means of identification

Product number -
Other names n-Nonacosanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4250-38-8 SDS

4250-38-8Downstream Products

4250-38-8Relevant articles and documents

C-GLYCOLIPIDS WITH ENHANCED TH-1 PROFILE

-

Page/Page column 37, (2008/06/13)

The invention is directed to novel synthetic C-glycolipids that selectively induce a ThI -type immune response characterized by enhanced IL- 12 secretion and increased activation of dendritic cells. The compounds of the invention are thereby useful in treating infections, cancers, cell proliferative disorders, and autoimmune diseases, both directly and as adjuvants.

Photosensitive Monolayers. Photochemistry of Long-Chain Diazo and Azide Compounds at the Air-Water Interface

Holden, David A.,Ringsdorf, Helmut,Haubs, Michael

, p. 4531 - 4536 (2007/10/02)

The photochemistry of a number of surface-active diazo and azide compounds was investigated in monolayers at the air-water boundary.Irradiation of long-chain α-diazo ketones with ultraviolet light leads to rapid loss of nitrogen.The resulting ketenes react with the subphase to generate carboxylic acids (photochemical Arndt-Eistert reaction) and dimerize to give β-lactones as side-products.A long-chain diester of 2-diazopropanedioic acid loses nitrogen and adds water, yielding the diester of 2-hydroxypropanedioic acid. α-Azido ketones split off nitrogen and the resulting isocyanates react with water (photoche mical Curtius reaction) and undergo further degradation to give complex product mixtures.These reactions lead to pronounced changes in the spreading behavior of the monolayers.Depending on functional group, chain length, substrate pH, and temperature it is possible to achieve changes in compressibility and collapse pressure, disappearance of expanded phases, collapse of monolayers to give oily films, or disappearance of monolayers by dissolution in the subphase.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 4250-38-8